Canonical Allele Identifier: CA394382869

Gene: PKD1

Linked Data

• dbSNP Id: rs906594578
• gnomAD v2: 16-2161614-C-A
• MyVariant Identifiers: chr16:g.2161614C>A (hg19) ; chr16:g.2111613C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.2111613C>A , CM000678.2:g.2111613C>A	GRCh38
NC_000016.9:g.2161614C>A , CM000678.1:g.2161614C>A	GRCh37
NC_000016.8:g.2101615C>A	NCBI36
NG_008617.1:g.29286G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262304.9:c.3554G>T MANE Select	ENSP00000262304.4:p.Gly1185Val
ENST00000262304.8:c.3554G>T	ENSP00000262304.4:p.Gly1185Val
ENST00000415938.7:n.310+727G>T
ENST00000423118.5:c.3554G>T	ENSP00000399501.1:p.Gly1185Val
ENST00000468674.5:n.430+727G>T
ENST00000469241.2:n.504G>T
ENST00000483024.1:c.233+203G>T
ENST00000483731.5:n.790+727G>T
ENST00000488185.2:c.473-3255G>T
ENST00000565639.6:n.773+727G>T
ENST00000568591.5:c.2226+727G>T	ENSP00000457162.1:n.2226+727G>T
ENST00000569983.5:n.421+727G>T
NM_000296.3:c.3554G>T	NP_000287.3:p.Gly1185Val
NM_001009944.2:c.3554G>T	NP_001009944.2:p.Gly1185Val
XM_005255370.2:c.509G>T	XP_005255427.1:p.Gly170Val
XM_011522525.1:c.3632G>T	XP_011520827.1:p.Gly1211Val
XM_011522526.1:c.3632G>T	XP_011520828.1:p.Gly1211Val
XM_011522527.1:c.3632G>T	XP_011520829.1:p.Gly1211Val
XM_011522528.1:c.3608G>T	XP_011520830.1:p.Gly1203Val
XM_011522529.1:c.3608G>T	XP_011520831.1:p.Gly1203Val
XM_011522530.1:c.3578G>T	XP_011520832.1:p.Gly1193Val
XM_011522531.1:c.3560G>T	XP_011520833.1:p.Gly1187Val
XM_011522532.1:c.3506G>T	XP_011520834.1:p.Gly1169Val
XM_011522533.1:c.3425G>T	XP_011520835.1:p.Gly1142Val
XM_011522534.1:c.3368G>T	XP_011520836.1:p.Gly1123Val
XM_011522535.1:c.1454G>T	XP_011520837.1:p.Gly485Val
XM_011522536.1:c.3632G>T	XP_011520838.1:p.Gly1211Val
XM_011522537.1:c.632G>T	XP_011520839.1:p.Gly211Val
XR_932867.1:n.3647G>T
XR_932868.1:n.3647G>T
XR_932869.1:n.3647G>T
XR_932870.1:n.3647G>T
XM_005255370.3:c.509G>T	XP_005255427.1:p.Gly170Val
XM_011522528.3:c.3608G>T	XP_011520830.1:p.Gly1203Val
XM_011522529.2:c.3608G>T	XP_011520831.1:p.Gly1203Val
XM_011522537.2:c.632G>T	XP_011520839.1:p.Gly211Val
XM_024450298.1:c.3674G>T	XP_024306066.1:p.Gly1225Val
XM_024450299.1:c.3602G>T	XP_024306067.1:p.Gly1201Val
XM_024450300.1:c.3464G>T	XP_024306068.1:p.Gly1155Val
XM_024450301.1:c.1550G>T	XP_024306069.1:p.Gly517Val
NM_000296.4:c.3554G>T	NP_000287.4:p.Gly1185Val
NM_001009944.3:c.3554G>T MANE Select	NP_001009944.3:p.Gly1185Val